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Formulation and Evaluation of Trifluoperazine HC1 as rectal suppositories by using different types of surfactants in Cocoa butter

机译:通过在可可脂中使用不同类型的表面活性剂作为直肠栓剂的三氟吡咯烷酮HC1的制剂和评价

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摘要

Simple and common materials such as cocoa butter and different types of surfactants such as span 60, tween80and PEG 400 were used to formulate rectal suppositories to deliver hydrophilic drug the trifluoperazineHCl. At 10% w/w PEG 400, the best prolonged release of trifluoperazine was obtained and this was returned to the emulsion formation between the PEG 400 and cocoa butter. This was proved by FTIR study which showed interactions of hydrogen bonds between carbonyl group of the triglyceride of cocoa butter and the hydroxyl group of PEG 400. Also, FTIR study showed trifluoperazine molecules were bonded to PEG 400 molecules as these bonds led trifluoperazine to be captured within the PEG 400 that representing the aqueous internal phase of presumed emulsion in the suppository. DSC test support this concept by showing a complete disappearance of trifluoprazine peaks in the thermograms of the suppositories that loaded with the trifluoperazine.
机译:使用诸如可可脂和不同类型的表面活性剂如Cocoa黄油和不同类型的表面活性剂,如跨度60,Tween80和PEG 400用于制备直肠栓剂,以提供亲水性药物TRIFLOPERAZINEHCL。 在10%w / w peg 400中,获得了最佳的三氟吡嗪的延长释放,将其返回到PEG 400和可可脂之间的乳液形成。 通过FTIR研究证明了,其显示在可可脂蛋白质的甘油酯和PEG 400的羟基之间的羰基与羟基之间的相互作用。此外,由于这些键将三氟吡嗪键合在PEG 400分子中,FTIR研究显示了三氟吡嗪分子。 在PEG 400内,表示栓剂中假定乳液的含水内部相。 DSC测试通过显示与三氟吡嗪的栓剂的热量点中的三氟唑嗪峰的完全消失,支持这种概念。

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